| Document Date: 2014-10-14 08:15:01
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Company Infectious / Disclaimer There / Rare / / / MedicalCondition Cutis laxa / Rare systemic and rheumatologic disease / parasitic myopathies / Neoplasms / group Infectious / congenital sensorineural deafness / rare diseases / Vasculitides / Joubert syndrome / phosphocalcic metabolism disorders / Dysostoses / Tietz syndrome / Rare endocrine disease / neurologic diseases / several diseases / systemic and rheumatologic diseases / Ocular albinism / Ectodermal dysplasias / Usher syndrome / papillomas / rheumatologic disease / deafness / disorder / endocrine tumours / endocrine disease / Angio-osteohypertrophic syndrome / clinical syndrome / Langerhans cell histiocytoses / late-onset sensorineural deafness / vitiligo / ORPHA93419 Rare bone disease / malignant tumours / benign tumours / specific diseases / surgical cardiac disease / disease / neoplasm / Rare neurologic disease / oncologic disease / odontologic disease / Non-histaminic angioedemas / Waardenburg syndrome / Neurofibromatosis / nephrotic syndrome / every rare disease / Inherited epidermolysis bullosa / bone diseases / Primary lipodystrophies / malformation syndrome / Neurovascular diseases / related disorders / hepatic failure / Diseases / Rare skin disease / infectious myosites / Albinism - deafness syndrome / carcinoid tumours / Infectious diseases / endocrine diseases / Ichthyoses / Inborn errors of metabolism / metabolic disease / contractures / Primary bone dysplasias / Amyloidoses / Deafblind hypopigmentation syndrome / infectious disease / skin diseases / syndrome / disorders / / Organization World Health Organization / / Person Julie Christ / Ana Rath / Bertrand Bellet / / Position Editor / dedicated information scientist / General / Usher / / URL www.orpha.net / http /
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September[removed]LINEARIZATION RULES FOR ORPHANET CLASSIFICATIONS Procedural document